The transformations occurring in the sub-stoichiometric Ti(C,N) – W - Al system
processed by high energy ball mill were investigated. The milling parameters included
the milling time and the temperature comprising milling at subzero temperature and
above 25°C. Two sub-stoichiometric Ti(C,N) stocks were selected, the Ti(C0.5N0.05)
containing more interstitial elements than the Ti(C0.5N0.5)0.6.The transformation stages
and mechanisms of alloying are discussed with respect to the changes in crystal structures
of the powder constituents. The milling atmosphere had an effect on the lattice strain of
milled products, and hence on the kinetics of solid state dissolution between the powder
constituents, but it did not affect the fracturing process.
The release of the stored crystallite lattice strain energy was the major determinant in
mechanical alloying, with particle size reduction playing a necessary, but less significant
role. The strain energy and the fine particle size contributed to the increased chemical reactivity with oxygen of the powders milled for shorter times. The affinity of the
powders with oxygen decreased after W dissolution in Ti(C,N), and the subsequent
decrease in lattice strains.
The annealing behaviour of Ti(C0.5N0.05) - 40wt% W and Ti(C0.5N0.5)0.6 - 40wt% W
mechanically alloyed powders were investigated using XRD, TEM, SEM and DTA
techniques. It was observed that the reaction start and finish temperatures between
constituents were lower in the system that had higher residual lattice strains after milling.
The compositions of the intermetallic compounds and the solid solutions formed were
dependent on the milling conditions and the annealing temperature. Thermal alloying was
observed during annealing of Ti(C0.5N0.05) - 40wt% W mechanically alloyed products,
whereas de-mixing of W-rich phases from the metastable solid solution occurred during
annealing of the Ti(C0.5N0.5)0.6 - 40wt% W milled powders.
The effects of Al addition and milling at subzero temperatures on the transformation of
Ti(C0.5N0.05)-W powder mixtures were investigated. Addition of Al powder improved the
kinetics of solid solution between powder constituents. The effect of Al was ascribed to
the increase of lattice strain during short milling time followed of relaxation at longer
time, and to the fast diffusion of atoms. Also, it was noticed that the high viscosity of the
process control agent could inhibit the alloying process.
Multiple three-component compounds could be formed. Aluminium preferably reacted
with tungsten. The W(Al,C) and W(Al,Ti) formed were stable, thus solubility of W in
Ti(C0.5N0.05) in the presence of Al was limited.
The evolution of the morphologies of Ti(C,N)-W mixtures show that fracturing of hard
particles dominated in the early stage of milling in the absence of Al, whereas with Al,
plastic deformation of particles and cold welding of Ti(C,N) and W particles by the
softer Al prevailed at the same time.
Longer milling time improved the homogeneity and the formation of nanostructured
binder pools in the sintered products. Lower oxygen contents in sintered PcBN were
achieved by mechanically alloying Ti(C,N), W and Al in the high energy ball milling
stage. Low level of Co in the infiltration layer was also achieved when sintering PcBN
with this type of binder. A link was established between the addition of Al at the attrition
milling stage and high oxygen content in the sintered PcBN, thus should be avoided.
The pressure and temperature applied during sintering or annealing had a strong effect on
the compositions and the crystal structures of the phases formed in the mechanically
alloyed binder. The lattice strains of the binder and the PcBN were higher in the sintered
materials prepared with the Ti(C0.5N0.5)0.6-W binder than in those made using the
Ti(C0.5N0.05)-W alloys.
Identifer | oai:union.ndltd.org:netd.ac.za/oai:union.ndltd.org:wits/oai:wiredspace.wits.ac.za:10539/11177 |
Date | 27 January 2012 |
Creators | Kasonde, Maweja. |
Source Sets | South African National ETD Portal |
Language | English |
Detected Language | English |
Type | Thesis |
Format | application/pdf, application/pdf, application/pdf |
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